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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704520Generated: October 30, 2026

Dimethyl Sulfide → HCID 14700143, compound

https://huagongshe.com/reaction/704520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
ReactantDimethyl SulfateHCID 6497—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 14700147HCID 14700147—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 14700143HCID 1470014380.2%

Reaction Conditions

Temperature20 °C

Reaction Steps

21 g (0.17 mol) of dimethyl sulphate are added dropwise with stirring at 20° C. to a solution of 10.5 g (0.17 mol) of dimethyl sulphide in 100 ml of acetonitrile. After standing for 2 days at 20° C., 9.2 g (0.17 mol) of sodium methoxide is added to this solution, the mixture is stirred for 30 minutes at 20° C. and then 29 g (0.09 mol) of 4-chlorophenoxymethyl 1-(4-chlorobenzyl)cycloprop-1-yl ketone are added. After stirring for 16 hours at 20° C., the reaction mixture is poured into water and the mixture is extracted with methylene chloride. The organic phase is washed with water, dried over magnesium sulphate and concentrated under reduced pressure. 25.2 g (80% of theory) of 2-(4-chlorophenoxymethyl)-2-[(4-chlorobenzyl)cycloprop-1-yl]-oxirane are obtained in the form of a colorless oil which is employed for further synthesis without additional purification. ##STR14##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04988383
Source datasetuspto-grants-1991_01
ORD IDord-2289cffa67684c8cbffc6fd925982417
Source noteuspto-grants-1991_01